Distinct genetic architecture of coronary heart disease in dyslipidemia patients

Abstract Background Mutations of LDLR, APOB and PCSK9 have been well-established to cause hypercholesterolemia while the pathogenic effects of LPL has been confirmed by cohorts and functional studies in hypertriglyceridemia. However, these mutations do not fully account for all dyslipidemia, and it...

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מידע ביבליוגרפי

Principais autores:	Man Huang, Xiuli Song, Shuni Zhou, Haiyan Zhang, Lijuan He, Yanghui Chen, Guangzhi Chen, Hu Ding, Jiangang Jiang, Yan Wang, Dao Wen Wang, Yang Sun, Hong Wang
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	BMC 2026-05-01
סדרה:	BMC Medical Genomics
נושאים:	Hypercholesterolemia Hypertriglyceridemia Whole exome sequencing Coronary heart disease LDLR APOB
גישה מקוונת:	https://doi.org/10.1186/s12920-026-02388-5
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